Canonical Allele Identifier: CA2187824588

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749791C= , CM000677.2:g.74749791C=	GRCh38
NC_000015.9:g.75042132C= , CM000677.1:g.75042132C=	GRCh37
NC_000015.8:g.72829185C=	NCBI36
NG_008431.1:g.32250C=
NG_008431.2:g.32250C=
NG_061543.1:g.5947C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.53C= MANE Select	ENSP00000342007.4:p.Ser18=
ENST00000343932.4:c.53C=	ENSP00000342007.4:p.Ser18=
NM_000761.4:c.53C=	NP_000752.2:p.Ser18=
NM_000761.5:c.53C= MANE Select	NP_000752.2:p.Ser18=